UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23416034C>A | CA389037345 | MHRT,MYH7 | c.4923G>T (p.Lys1641Asn) n.295C>A | |
| 14 | g.23416034C>G | CA389037346 | MHRT,MYH7 | c.4923G>C (p.Lys1641Asn) n.295C>G | |
| 14 | g.23416034C>T | CA485766466 | MHRT,MYH7 | c.4923G>A (p.Lys1641=) n.295C>T | |
| 14 | g.23416035T>A | CA389037347 | MHRT,MYH7 | c.4922A>T (p.Lys1641Met) n.296T>A | |
| 14 | g.23416035T>C | CA389037348 | MHRT,MYH7 | c.4922A>G (p.Lys1641Arg) n.296T>C | |
| 14 | g.23416035T>G | CA389037349 | MHRT,MYH7 | c.4922A>C (p.Lys1641Thr) n.296T>G | gnomAD v4 |
| 14 | g.23416036T>A | CA389037350 | MHRT,MYH7 | c.4921A>T (p.Lys1641Ter) n.297T>A | |
| 14 | g.23416036T>C | CA389037351 | MHRT,MYH7 | c.4921A>G (p.Lys1641Glu) n.297T>C | |
| 14 | g.23416036T>G | CA389037352 | MHRT,MYH7 | c.4921A>C (p.Lys1641Gln) n.297T>G | |
| 14 | g.23416037C>A | CA389037353 | MHRT,MYH7 | c.4920G>T (p.Gln1640His) n.298C>A | COSMIC |
| 14 | g.23416037C= | CA2123465077 | MHRT,MYH7 | c.4920G= (p.Gln1640=) n.298C= | |
| 14 | g.23416037C>G | CA389037354 | MHRT,MYH7 | c.4920G>C (p.Gln1640His) n.298C>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416037C>T | CA485766467 | MHRT,MYH7 | c.4920G>A (p.Gln1640=) n.298C>T | dbSNP |
| 14 | g.23416038T>A | CA044243 | MHRT,MYH7 | c.4919A>T (p.Gln1640Leu) n.299T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416038T>C | CA389037355 | MHRT,MYH7 | c.4919A>G (p.Gln1640Arg) n.299T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416038T>G | CA389037356 | MHRT,MYH7 | c.4919A>C (p.Gln1640Pro) n.299T>G | ClinVar dbSNP |
| 14 | g.23416038T= | CA2123465082 | MHRT,MYH7 | c.4919A= (p.Gln1640=) n.299T= | |
| 14 | g.23416039G>A | CA389037359 | MHRT,MYH7 | c.4918C>T (p.Gln1640Ter) n.300G>A | ClinVar |
| 14 | g.23416039G>C | CA389037358 | MHRT,MYH7 | c.4918C>G (p.Gln1640Glu) n.300G>C | |
| 14 | g.23416039G>T | CA389037357 | MHRT,MYH7 | c.4918C>A (p.Gln1640Lys) n.300G>T | |
| 14 | g.23416040G>A | CA485766469 | MHRT,MYH7 | c.4917C>T (p.Ala1639=) n.301G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416040G>C | CA485766470 | MHRT,MYH7 | c.4917C>G (p.Ala1639=) n.301G>C | |
| 14 | g.23416040G= | CA2123465087 | MHRT,MYH7 | c.4917C= (p.Ala1639=) n.301G= | |
| 14 | g.23416040G>T | CA485766472 | MHRT,MYH7 | c.4917C>A (p.Ala1639=) n.301G>T | |
| 14 | g.23416041G>A | CA389037360 | MHRT,MYH7 | c.4916C>T (p.Ala1639Val) n.302G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416041G>C | CA389037361 | MHRT,MYH7 | c.4916C>G (p.Ala1639Gly) n.302G>C | |
| 14 | g.23416041G= | CA2123465093 | MHRT,MYH7 | c.4916C= (p.Ala1639=) n.302G= | |
| 14 | g.23416041G>T | CA389037362 | MHRT,MYH7 | c.4916C>A (p.Ala1639Asp) n.302G>T | |
| 14 | g.23416042C>A | CA389037363 | MHRT,MYH7 | c.4915G>T (p.Ala1639Ser) n.303C>A | dbSNP |
| 14 | g.23416042C= | CA2123465095 | MHRT,MYH7 | c.4915G= (p.Ala1639=) n.303C= | |
| 14 | g.23416042C>G | CA389037364 | MHRT,MYH7 | c.4915G>C (p.Ala1639Pro) n.303C>G | |
| 14 | g.23416042C>T | CA248944 | MHRT,MYH7 | c.4915G>A (p.Ala1639Thr) n.303C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416043C>A | CA389037365 | MHRT,MYH7 | c.4914G>T (p.Glu1638Asp) n.304C>A | |
| 14 | g.23416043C= | CA2123465105 | MHRT,MYH7 | c.4914G= (p.Glu1638=) n.304C= | |
| 14 | g.23416043C>G | CA389037366 | MHRT,MYH7 | c.4914G>C (p.Glu1638Asp) n.304C>G | |
| 14 | g.23416043C>T | CA044233 | MHRT,MYH7 | c.4914G>A (p.Glu1638=) n.304C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416044T>A | CA389037367 | MHRT,MYH7 | c.4913A>T (p.Glu1638Val) n.305T>A | |
| 14 | g.23416044T>C | CA389037368 | MHRT,MYH7 | c.4913A>G (p.Glu1638Gly) n.305T>C | |
| 14 | g.23416044T>G | CA389037369 | MHRT,MYH7 | c.4913A>C (p.Glu1638Ala) n.305T>G | |
| 14 | g.23416044_23416046delinsCGAGGCCCAGAAGCCGA | CA2825002210 | MHRT,MYH7 | c.4911_4913delinsTCGGCTTCTGGGCCTCG (p.Glu1638ArgfsTer18) n.305_307delinsCGAGGCCCAGAAGCCGA | ClinVar |
| 14 | g.23416045C>A | CA389037371 | MHRT,MYH7 | c.4912G>T (p.Glu1638Ter) n.306C>A | |
| 14 | g.23416045C= | CA2123465106 | MHRT,MYH7 | c.4912G= (p.Glu1638=) n.306C= | |
| 14 | g.23416045C>G | CA389037372 | MHRT,MYH7 | c.4912G>C (p.Glu1638Gln) n.306C>G | |
| 14 | g.23416045C>T | CA389037370 | MHRT,MYH7 | c.4912G>A (p.Glu1638Lys) n.306C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416046G>A | CA015462 | MHRT,MYH7 | c.4911C>T (p.Ala1637=) n.307G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416046G>C | CA485766475 | MHRT,MYH7 | c.4911C>G (p.Ala1637=) n.307G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416046G= | CA2123465110 | MHRT,MYH7 | c.4911C= (p.Ala1637=) n.307G= | |
| 14 | g.23416046G>T | CA485766474 | MHRT,MYH7 | c.4911C>A (p.Ala1637=) n.307G>T | |
| 14 | g.23416047G>A | CA389037373 | MHRT,MYH7 | c.4910C>T (p.Ala1637Val) n.308G>A | COSMIC |
| 14 | g.23416047G>C | CA389037374 | MHRT,MYH7 | c.4910C>G (p.Ala1637Gly) n.308G>C | |
| 14 | g.23416047G>T | CA389037375 | MHRT,MYH7 | c.4910C>A (p.Ala1637Asp) n.308G>T | |
| 14 | g.23416048C>A | CA389037376 | MHRT,MYH7 | c.4909G>T (p.Ala1637Ser) n.309C>A | |
| 14 | g.23416048C= | CA2123465118 | MHRT,MYH7 | c.4909G= (p.Ala1637=) n.309C= | |
| 14 | g.23416048C>G | CA389037377 | MHRT,MYH7 | c.4909G>C (p.Ala1637Pro) n.309C>G | ClinVar dbSNP |
| 14 | g.23416048C>T | CA015454 | MHRT,MYH7 | c.4909G>A (p.Ala1637Thr) n.309C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416049G>A | CA044195 | MHRT,MYH7 | c.4908C>T (p.Ala1636=) n.310G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416049G>C | CA485766476 | MHRT,MYH7 | c.4908C>G (p.Ala1636=) n.310G>C | |
| 14 | g.23416049G= | CA2123465125 | MHRT,MYH7 | c.4908C= (p.Ala1636=) n.310G= | |
| 14 | g.23416049G>T | CA485766477 | MHRT,MYH7 | c.4908C>A (p.Ala1636=) n.310G>T | |
| 14 | g.23416050G>A | CA389037378 | MHRT,MYH7 | c.4907C>T (p.Ala1636Val) n.311G>A | ClinVar dbSNP |
| 14 | g.23416050G>C | CA389037379 | MHRT,MYH7 | c.4907C>G (p.Ala1636Gly) n.311G>C | |
| 14 | g.23416050G= | CA2123465129 | MHRT,MYH7 | c.4907C= (p.Ala1636=) n.311G= | |
| 14 | g.23416050G>T | CA389037380 | MHRT,MYH7 | c.4907C>A (p.Ala1636Asp) n.311G>T | |
| 14 | g.23416051C>A | CA389037381 | MHRT,MYH7 | c.4906G>T (p.Ala1636Ser) n.312C>A | |
| 14 | g.23416051C= | CA2123465138 | MHRT,MYH7 | c.4906G= (p.Ala1636=) n.312C= | |
| 14 | g.23416051C>G | CA015450 | MHRT,MYH7 | c.4906G>C (p.Ala1636Pro) n.312C>G | ClinVar dbSNP |
| 14 | g.23416051C>T | CA389037382 | MHRT,MYH7 | c.4906G>A (p.Ala1636Thr) n.312C>T | COSMIC |
| 14 | g.23416052C>A | CA389037383 | MHRT,MYH7 | c.4905G>T (p.Met1635Ile) n.313C>A | |
| 14 | g.23416052C>G | CA389037385 | MHRT,MYH7 | c.4905G>C (p.Met1635Ile) n.313C>G | |
| 14 | g.23416052C>T | CA389037384 | MHRT,MYH7 | c.4905G>A (p.Met1635Ile) n.313C>T | |
| 14 | g.23416053A= | CA2123465154 | MHRT,MYH7 | c.4904T= (p.Met1635=) n.314A= | |
| 14 | g.23416053A>C | CA389037386 | MHRT,MYH7 | c.4904T>G (p.Met1635Arg) n.314A>C | |
| 14 | g.23416053A>G | CA015442 | MHRT,MYH7 | c.4904T>C (p.Met1635Thr) n.314A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416053A>T | CA389037387 | MHRT,MYH7 | c.4904T>A (p.Met1635Lys) n.314A>T | |
| 14 | g.23416054T>A | CA389037388 | MHRT,MYH7 | c.4903A>T (p.Met1635Leu) n.315T>A | dbSNP |
| 14 | g.23416054T>C | CA044177 | MHRT,MYH7 | c.4903A>G (p.Met1635Val) n.315T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416054T>G | CA389037389 | MHRT,MYH7 | c.4903A>C (p.Met1635Leu) n.315T>G | |
| 14 | g.23416054T= | CA2123465162 | MHRT,MYH7 | c.4903A= (p.Met1635=) n.315T= | |
| 14 | g.23416055G>A | CA485766485 | MHRT,MYH7 | c.4902C>T (p.Arg1634=) n.316G>A | |
| 14 | g.23416055G>C | CA485766486 | MHRT,MYH7 | c.4902C>G (p.Arg1634=) n.316G>C | |
| 14 | g.23416055G>T | CA485766487 | MHRT,MYH7 | c.4902C>A (p.Arg1634=) n.316G>T | |
| 14 | g.23416056C>A | CA389037390 | MHRT,MYH7 | c.4901G>T (p.Arg1634Leu) n.317C>A | ClinVar dbSNP |
| 14 | g.23416056C= | CA2123465167 | MHRT,MYH7 | c.4901G= (p.Arg1634=) n.317C= | |
| 14 | g.23416056C>G | CA389037391 | MHRT,MYH7 | c.4901G>C (p.Arg1634Pro) n.317C>G | |
| 14 | g.23416056C>T | CA077498 | MHRT,MYH7 | c.4901G>A (p.Arg1634His) n.317C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416056_23416057delinsCG | CA2123465169 | MHRT,MYH7 | c.4900_4901delinsCG (p.Arg1634=) n.317_318delinsCG | |
| 14 | g.23416057G>A | CA015436 | MHRT,MYH7 | c.4900C>T (p.Arg1634Cys) n.318G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416057G>C | CA389037392 | MHRT,MYH7 | c.4900C>G (p.Arg1634Gly) n.318G>C | |
| 14 | g.23416057G= | CA2123465183 | MHRT,MYH7 | c.4900C= (p.Arg1634=) n.318G= | |
| 14 | g.23416057G>T | CA389037393 | MHRT,MYH7 | c.4900C>A (p.Arg1634Ser) n.318G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416058del | CA613317699 | MHRT,MYH7 | c.4900del (p.Arg1634AlafsTer17) n.319del | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416058G>A | CA257810449 | MHRT,MYH7 | c.4899C>T (p.Asn1633=) n.319G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416058G>C | CA389037394 | MHRT,MYH7 | c.4899C>G (p.Asn1633Lys) n.319G>C | |
| 14 | g.23416058G= | CA2123465190 | MHRT,MYH7 | c.4899C= (p.Asn1633=) n.319G= | |
| 14 | g.23416058G>T | CA389037395 | MHRT,MYH7 | c.4899C>A (p.Asn1633Lys) n.319G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416059T>A | CA389037396 | MHRT,MYH7 | c.4898A>T (p.Asn1633Ile) n.320T>A | |
| 14 | g.23416059T>C | CA389037397 | MHRT,MYH7 | c.4898A>G (p.Asn1633Ser) n.320T>C | dbSNP |
| 14 | g.23416059T>G | CA389037398 | MHRT,MYH7 | c.4898A>C (p.Asn1633Thr) n.320T>G | |
| 14 | g.23416059T= | CA2123465198 | MHRT,MYH7 | c.4898A= (p.Asn1633=) n.320T= | |
| 14 | g.23416060T>A | CA389037399 | MHRT,MYH7 | c.4897A>T (p.Asn1633Tyr) n.321T>A | |
| 14 | g.23416060T>C | CA044154 | MHRT,MYH7 | c.4897A>G (p.Asn1633Asp) n.321T>C | ClinVar dbSNP ExAC gnomAD v2 |
| 14 | g.23416060T>G | CA389037400 | MHRT,MYH7 | c.4897A>C (p.Asn1633His) n.321T>G | |
| 14 | g.23416060T= | CA2123465201 | MHRT,MYH7 | c.4897A= (p.Asn1633=) n.321T= | |
| 14 | g.23416061G>A | CA485766490 | MHRT,MYH7 | c.4896C>T (p.Ala1632=) n.322G>A | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416061G>C | CA485766491 | MHRT,MYH7 | c.4896C>G (p.Ala1632=) n.322G>C | |
| 14 | g.23416061G= | CA2123465205 | MHRT,MYH7 | c.4896C= (p.Ala1632=) n.322G= | |
| 14 | g.23416061G>T | CA044135 | MHRT,MYH7 | c.4896C>A (p.Ala1632=) n.322G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416062G>A | CA389037401 | MHRT,MYH7 | c.4895C>T (p.Ala1632Val) n.323G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416062G>C | CA389037402 | MHRT,MYH7 | c.4895C>G (p.Ala1632Gly) n.323G>C | |
| 14 | g.23416062G= | CA2123465210 | MHRT,MYH7 | c.4895C= (p.Ala1632=) n.323G= | |
| 14 | g.23416062G>T | CA389037403 | MHRT,MYH7 | c.4895C>A (p.Ala1632Asp) n.323G>T | ClinVar dbSNP |
| 14 | g.23416063C>A | CA389037404 | MHRT,MYH7 | c.4894G>T (p.Ala1632Ser) n.324C>A | ClinVar |
| 14 | g.23416063C= | CA2123465216 | MHRT,MYH7 | c.4894G= (p.Ala1632=) n.324C= | |
| 14 | g.23416063C>G | CA389037405 | MHRT,MYH7 | c.4894G>C (p.Ala1632Pro) n.324C>G | ClinVar dbSNP |
| 14 | g.23416063C>T | CA044125 | MHRT,MYH7 | c.4894G>A (p.Ala1632Thr) n.324C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416064G>A | CA044116 | MHRT,MYH7 | c.4893C>T (p.His1631=) n.325G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416064G>C | CA389037407 | MHRT,MYH7 | c.4893C>G (p.His1631Gln) n.325G>C | |
| 14 | g.23416064G= | CA2123465223 | MHRT,MYH7 | c.4893C= (p.His1631=) n.325G= | |
| 14 | g.23416064G>T | CA389037406 | MHRT,MYH7 | c.4893C>A (p.His1631Gln) n.325G>T | |
| 14 | g.23416065T>A | CA389037408 | MHRT,MYH7 | c.4892A>T (p.His1631Leu) n.326T>A | |
| 14 | g.23416065T>C | CA389037409 | MHRT,MYH7 | c.4892A>G (p.His1631Arg) n.326T>C | |
| 14 | g.23416065T>G | CA389037410 | MHRT,MYH7 | c.4892A>C (p.His1631Pro) n.326T>G | |
| 14 | g.23416066G>A | CA389037411 | MHRT,MYH7 | c.4891C>T (p.His1631Tyr) n.327G>A | dbSNP |
| 14 | g.23416066G>C | CA389037412 | MHRT,MYH7 | c.4891C>G (p.His1631Asp) n.327G>C | |
| 14 | g.23416066G>T | CA389037413 | MHRT,MYH7 | c.4891C>A (p.His1631Asn) n.327G>T | |
| 14 | g.23416067G>A | CA485766492 | MHRT,MYH7 | c.4890C>T (p.Ser1630=) n.328G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416067G>C | CA389037414 | MHRT,MYH7 | c.4890C>G (p.Ser1630Arg) n.328G>C | |
| 14 | g.23416067G= | CA2123465232 | MHRT,MYH7 | c.4890C= (p.Ser1630=) n.328G= | |
| 14 | g.23416067G>T | CA389037415 | MHRT,MYH7 | c.4890C>A (p.Ser1630Arg) n.328G>T | |
| 14 | g.23416071_23416075del | CA913184894 | MHRT,MYH7 | c.4886_4890del (p.Leu1629ProfsTer?) n.332_336del | |
| 14 | g.23416068C>A | CA389037416 | MHRT,MYH7 | c.4889G>T (p.Ser1630Ile) n.329C>A | |
| 14 | g.23416068C>G | CA389037417 | MHRT,MYH7 | c.4889G>C (p.Ser1630Thr) n.329C>G | |
| 14 | g.23416068C>T | CA389037418 | MHRT,MYH7 | c.4889G>A (p.Ser1630Asn) n.329C>T | |
| 14 | g.23416069T>A | CA389037419 | MHRT,MYH7 | c.4888A>T (p.Ser1630Cys) n.330T>A | |
| 14 | g.23416069T>C | CA389037420 | MHRT,MYH7 | c.4888A>G (p.Ser1630Gly) n.330T>C | |
| 14 | g.23416069T>G | CA389037421 | MHRT,MYH7 | c.4888A>C (p.Ser1630Arg) n.330T>G | |
| 14 | g.23416070G>A | CA485766493 | MHRT,MYH7 | c.4887C>T (p.Leu1629=) n.331G>A | |
| 14 | g.23416070G>C | CA485766494 | MHRT,MYH7 | c.4887C>G (p.Leu1629=) n.331G>C | |
| 14 | g.23416070G>T | CA485766495 | MHRT,MYH7 | c.4887C>A (p.Leu1629=) n.331G>T | |
| 14 | g.23416071A= | CA2123465249 | MHRT,MYH7 | c.4886T= (p.Leu1629=) n.332A= | |
| 14 | g.23416071A>C | CA389037423 | MHRT,MYH7 | c.4886T>G (p.Leu1629Arg) n.332A>C | |
| 14 | g.23416071A>G | CA207077 | MHRT,MYH7 | c.4886T>C (p.Leu1629Pro) n.332A>G | ClinVar dbSNP |
| 14 | g.23416071A>T | CA389037422 | MHRT,MYH7 | c.4886T>A (p.Leu1629His) n.332A>T | |
| 14 | g.23416072G>A | CA389037424 | MHRT,MYH7 | c.4885C>T (p.Leu1629Phe) n.333G>A | |
| 14 | g.23416072G>C | CA389037425 | MHRT,MYH7 | c.4885C>G (p.Leu1629Val) n.333G>C | |
| 14 | g.23416072G>T | CA389037426 | MHRT,MYH7 | c.4885C>A (p.Leu1629Ile) n.333G>T | |
| 14 | g.23416073C>A | CA389037427 | MHRT,MYH7 | c.4884G>T (p.Gln1628His) n.334C>A | |
| 14 | g.23416073C>G | CA389037428 | MHRT,MYH7 | c.4884G>C (p.Gln1628His) n.334C>G | |
| 14 | g.23416073C>T | CA485766496 | MHRT,MYH7 | c.4884G>A (p.Gln1628=) n.334C>T | |
| 14 | g.23416074T>A | CA389037429 | MHRT,MYH7 | c.4883A>T (p.Gln1628Leu) n.335T>A | |
| 14 | g.23416074T>C | CA389037430 | MHRT,MYH7 | c.4883A>G (p.Gln1628Arg) n.335T>C | |
| 14 | g.23416074T>G | CA389037431 | MHRT,MYH7 | c.4883A>C (p.Gln1628Pro) n.335T>G | |
| 14 | g.23416075G>A | CA389037432 | MHRT,MYH7 | c.4882C>T (p.Gln1628Ter) n.336G>A | |
| 14 | g.23416075G>C | CA389037434 | MHRT,MYH7 | c.4882C>G (p.Gln1628Glu) n.336G>C | |
| 14 | g.23416075G= | CA2123465255 | MHRT,MYH7 | c.4882C= (p.Gln1628=) n.336G= | |
| 14 | g.23416075G>T | CA389037433 | MHRT,MYH7 | c.4882C>A (p.Gln1628Lys) n.336G>T | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416076G>A | CA485766497 | MHRT,MYH7 | c.4881C>T (p.Ile1627=) n.337G>A | |
| 14 | g.23416076G>C | CA389037435 | MHRT,MYH7 | c.4881C>G (p.Ile1627Met) n.337G>C | |
| 14 | g.23416076G= | CA2123465256 | MHRT,MYH7 | c.4881C= (p.Ile1627=) n.337G= | |
| 14 | g.23416076G>T | CA485766498 | MHRT,MYH7 | c.4881C>A (p.Ile1627=) n.337G>T | dbSNP |
| 14 | g.23416077A= | CA2123465258 | MHRT,MYH7 | c.4880T= (p.Ile1627=) n.338A= | |
| 14 | g.23416077A>C | CA389037436 | MHRT,MYH7 | c.4880T>G (p.Ile1627Ser) n.338A>C | ClinVar dbSNP |
| 14 | g.23416077A>G | CA389037437 | MHRT,MYH7 | c.4880T>C (p.Ile1627Thr) n.338A>G | |
| 14 | g.23416077A>T | CA389037438 | MHRT,MYH7 | c.4880T>A (p.Ile1627Asn) n.338A>T | |
| 14 | g.23416078T>A | CA389037439 | MHRT,MYH7 | c.4879A>T (p.Ile1627Phe) n.339T>A | |
| 14 | g.23416078T>C | CA389037441 | MHRT,MYH7 | c.4879A>G (p.Ile1627Val) n.339T>C | |
| 14 | g.23416078T>G | CA389037440 | MHRT,MYH7 | c.4879A>C (p.Ile1627Leu) n.339T>G | ClinVar dbSNP |
| 14 | g.23416078T= | CA2123465261 | MHRT,MYH7 | c.4879A= (p.Ile1627=) n.339T= | |
| 14 | g.23416079C>A | CA389037442 | MHRT,MYH7 | c.4878G>T (p.Glu1626Asp) n.340C>A | |
| 14 | g.23416079C>G | CA389037443 | MHRT,MYH7 | c.4878G>C (p.Glu1626Asp) n.340C>G | |
| 14 | g.23416079C>T | CA485766499 | MHRT,MYH7 | c.4878G>A (p.Glu1626=) n.340C>T | |
| 14 | g.23416080T>A | CA389037444 | MHRT,MYH7 | c.4877A>T (p.Glu1626Val) n.341T>A | |
| 14 | g.23416080T>C | CA389037445 | MHRT,MYH7 | c.4877A>G (p.Glu1626Gly) n.341T>C | |
| 14 | g.23416080T>G | CA389037446 | MHRT,MYH7 | c.4877A>C (p.Glu1626Ala) n.341T>G | |
| 14 | g.23416081C>A | CA389037447 | MHRT,MYH7 | c.4876G>T (p.Glu1626Ter) n.342C>A | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416081C= | CA2123465264 | MHRT,MYH7 | c.4876G= (p.Glu1626=) n.342C= | |
| 14 | g.23416081C>G | CA389037448 | MHRT,MYH7 | c.4876G>C (p.Glu1626Gln) n.342C>G | |
| 14 | g.23416081C>T | CA389037449 | MHRT,MYH7 | c.4876G>A (p.Glu1626Lys) n.342C>T | ClinVar |
| 14 | g.23416082C>A | CA389037450 | MHRT,MYH7 | c.4875G>T (p.Met1625Ile) n.343C>A | |
| 14 | g.23416082C>G | CA389037451 | MHRT,MYH7 | c.4875G>C (p.Met1625Ile) n.343C>G | |
| 14 | g.23416082C>T | CA389037452 | MHRT,MYH7 | c.4875G>A (p.Met1625Ile) n.343C>T | |
| 14 | g.23416083A>C | CA389037453 | MHRT,MYH7 | c.4874T>G (p.Met1625Arg) n.344A>C | ClinVar |
| 14 | g.23416083A>G | CA389037455 | MHRT,MYH7 | c.4874T>C (p.Met1625Thr) n.344A>G | gnomAD v4 |
| 14 | g.23416083A>T | CA389037454 | MHRT,MYH7 | c.4874T>A (p.Met1625Lys) n.344A>T | |
| 14 | g.23416084T>A | CA389037456 | MHRT,MYH7 | c.4873A>T (p.Met1625Leu) n.345T>A | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416084T>C | CA389037458 | MHRT,MYH7 | c.4873A>G (p.Met1625Val) n.345T>C | |
| 14 | g.23416084T>G | CA389037457 | MHRT,MYH7 | c.4873A>C (p.Met1625Leu) n.345T>G | |
| 14 | g.23416084T= | CA2123465268 | MHRT,MYH7 | c.4873A= (p.Met1625=) n.345T= | |
| 14 | g.23416085C>A | CA389037459 | MHRT,MYH7 | c.4872G>T (p.Glu1624Asp) n.346C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416085C= | CA2123465272 | MHRT,MYH7 | c.4872G= (p.Glu1624=) n.346C= | |
| 14 | g.23416085C>G | CA389037460 | MHRT,MYH7 | c.4872G>C (p.Glu1624Asp) n.346C>G | |
| 14 | g.23416085C>T | CA044101 | MHRT,MYH7 | c.4872G>A (p.Glu1624=) n.346C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416086T>A | CA389037461 | MHRT,MYH7 | c.4871A>T (p.Glu1624Val) n.347T>A | |
| 14 | g.23416086T>C | CA389037462 | MHRT,MYH7 | c.4871A>G (p.Glu1624Gly) n.347T>C | |
| 14 | g.23416086T>G | CA389037463 | MHRT,MYH7 | c.4871A>C (p.Glu1624Ala) n.347T>G | gnomAD v4 |
| 14 | g.23416087C>A | CA389037464 | MHRT,MYH7 | c.4870G>T (p.Glu1624Ter) n.348C>A | |
| 14 | g.23416087C>G | CA389037465 | MHRT,MYH7 | c.4870G>C (p.Glu1624Gln) n.348C>G | COSMIC |
| 14 | g.23416087C>T | CA389037466 | MHRT,MYH7 | c.4870G>A (p.Glu1624Lys) n.348C>T | ClinVar dbSNP |
| 14 | g.23416088A= | CA2123465278 | MHRT,MYH7 | c.4869T= (p.Asn1623=) n.349A= | |
| 14 | g.23416088A>C | CA389037467 | MHRT,MYH7 | c.4869T>G (p.Asn1623Lys) n.349A>C | |
| 14 | g.23416088A>G | CA485766500 | MHRT,MYH7 | c.4869T>C (p.Asn1623=) n.349A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416088A>T | CA389037468 | MHRT,MYH7 | c.4869T>A (p.Asn1623Lys) n.349A>T | |
| 14 | g.23416089T>A | CA389037471 | MHRT,MYH7 | c.4868A>T (p.Asn1623Ile) n.350T>A | |
| 14 | g.23416089T>C | CA389037470 | MHRT,MYH7 | c.4868A>G (p.Asn1623Ser) n.350T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416089T>G | CA389037469 | MHRT,MYH7 | c.4868A>C (p.Asn1623Thr) n.350T>G | |
| 14 | g.23416089T= | CA2123465284 | MHRT,MYH7 | c.4868A= (p.Asn1623=) n.350T= | |
| 14 | g.23416090T>A | CA389037472 | MHRT,MYH7 | c.4867A>T (p.Asn1623Tyr) n.351T>A | |
| 14 | g.23416090T>C | CA389037473 | MHRT,MYH7 | c.4867A>G (p.Asn1623Asp) n.351T>C | |
| 14 | g.23416090T>G | CA389037474 | MHRT,MYH7 | c.4867A>C (p.Asn1623His) n.351T>G | |
| 14 | g.23416091G>A | CA485766501 | MHRT,MYH7 | c.4866C>T (p.Leu1622=) n.352G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416091G>C | CA485766502 | MHRT,MYH7 | c.4866C>G (p.Leu1622=) n.352G>C | |
| 14 | g.23416091G= | CA2123465289 | MHRT,MYH7 | c.4866C= (p.Leu1622=) n.352G= | |
| 14 | g.23416091G>T | CA485766503 | MHRT,MYH7 | c.4866C>A (p.Leu1622=) n.352G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416092A>C | CA389037475 | MHRT,MYH7 | c.4865T>G (p.Leu1622Arg) n.353A>C | |
| 14 | g.23416092A>G | CA389037476 | MHRT,MYH7 | c.4865T>C (p.Leu1622Pro) n.353A>G | |
| 14 | g.23416092A>T | CA389037477 | MHRT,MYH7 | c.4865T>A (p.Leu1622His) n.353A>T | gnomAD v4 |
| 14 | g.23416093G>A | CA015424 | MHRT,MYH7 | c.4864C>T (p.Leu1622Phe) n.354G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416093G>C | CA389037478 | MHRT,MYH7 | c.4864C>G (p.Leu1622Val) n.354G>C | |
| 14 | g.23416093G= | CA2123465295 | MHRT,MYH7 | c.4864C= (p.Leu1622=) n.354G= | |
| 14 | g.23416093G>T | CA389037479 | MHRT,MYH7 | c.4864C>A (p.Leu1622Ile) n.354G>T | |
| 14 | g.23416094G>A | CA485766504 | MHRT,MYH7 | c.4863C>T (p.Asp1621=) n.355G>A | ClinVar |
| 14 | g.23416094G>C | CA389037480 | MHRT,MYH7 | c.4863C>G (p.Asp1621Glu) n.355G>C | |
| 14 | g.23416094G>T | CA389037481 | MHRT,MYH7 | c.4863C>A (p.Asp1621Glu) n.355G>T | |
| 14 | g.23416095T>A | CA389037484 | MHRT,MYH7 | c.4862A>T (p.Asp1621Val) n.356T>A | |
| 14 | g.23416095T>C | CA389037483 | MHRT,MYH7 | c.4862A>G (p.Asp1621Gly) n.356T>C | |
| 14 | g.23416095T>G | CA389037482 | MHRT,MYH7 | c.4862A>C (p.Asp1621Ala) n.356T>G | dbSNP |
| 14 | g.23416095T= | CA2123465302 | MHRT,MYH7 | c.4862A= (p.Asp1621=) n.356T= | |
| 14 | g.23416096C>A | CA389037485 | MHRT,MYH7 | c.4861G>T (p.Asp1621Tyr) n.357C>A | |
| 14 | g.23416096C= | CA2123465303 | MHRT,MYH7 | c.4861G= (p.Asp1621=) n.357C= | |
| 14 | g.23416096C>G | CA389037486 | MHRT,MYH7 | c.4861G>C (p.Asp1621His) n.357C>G | |
| 14 | g.23416096C>T | CA044085 | MHRT,MYH7 | c.4861G>A (p.Asp1621Asn) n.357C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416097T>A | CA485766505 | MHRT,MYH7 | c.4860A>T (p.Gly1620=) n.358T>A | |
| 14 | g.23416097T>C | CA485766506 | MHRT,MYH7 | c.4860A>G (p.Gly1620=) n.358T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416097T>G | CA485766507 | MHRT,MYH7 | c.4860A>C (p.Gly1620=) n.358T>G | dbSNP |
| 14 | g.23416097T= | CA2123465307 | MHRT,MYH7 | c.4860A= (p.Gly1620=) n.358T= | |
| 14 | g.23416098C>A | CA389037487 | MHRT,MYH7 | c.4859G>T (p.Gly1620Val) n.359C>A | |
| 14 | g.23416098C>G | CA389037488 | MHRT,MYH7 | c.4859G>C (p.Gly1620Ala) n.359C>G | |
| 14 | g.23416098C>T | CA389037489 | MHRT,MYH7 | c.4859G>A (p.Gly1620Glu) n.359C>T | |
| 14 | g.23416099C>A | CA389037490 | MHRT,MYH7 | c.4858G>T (p.Gly1620Ter) n.360C>A | |
| 14 | g.23416099C>G | CA389037491 | MHRT,MYH7 | c.4858G>C (p.Gly1620Arg) n.360C>G | |
| 14 | g.23416099C>T | CA389037492 | MHRT,MYH7 | c.4858G>A (p.Gly1620Arg) n.360C>T | |
| 14 | g.23416100T>A | CA389037493 | MHRT,MYH7 | c.4857A>T (p.Glu1619Asp) n.361T>A | |
| 14 | g.23416100T>C | CA485766508 | MHRT,MYH7 | c.4857A>G (p.Glu1619=) n.361T>C | ClinVar dbSNP |
| 14 | g.23416100T>G | CA389037494 | MHRT,MYH7 | c.4857A>C (p.Glu1619Asp) n.361T>G | |
| 14 | g.23416100T= | CA2123465310 | MHRT,MYH7 | c.4857A= (p.Glu1619=) n.361T= | |
| 14 | g.23416101T>A | CA389037497 | MHRT,MYH7 | c.4856A>T (p.Glu1619Val) n.362T>A | |
| 14 | g.23416101T>C | CA389037496 | MHRT,MYH7 | c.4856A>G (p.Glu1619Gly) n.362T>C | |
| 14 | g.23416101T>G | CA389037495 | MHRT,MYH7 | c.4856A>C (p.Glu1619Ala) n.362T>G | |
| 14 | g.23416113_23416114insACTTCAGTCTGGAGCTGGGACAGGTCAGCATCCATCTTCTTCT | CA044072 | MHRT,MYH7 | c.4856_4857insTGCTGACCTGTCCCAGCTCCAGACTGAAGTAGAAGAAGATGGA (p.Glu1619AspfsTer20) n.374_375insACTTCAGTCTGGAGCTGGGACAGGTCAGCATCCATCTTCTTCT | dbSNP ExAC |
| 14 | g.23416102C>A | CA389037498 | MHRT,MYH7 | c.4855G>T (p.Glu1619Ter) n.363C>A | |
| 14 | g.23416102C= | CA2123465321 | MHRT,MYH7 | c.4855G= (p.Glu1619=) n.363C= | |
| 14 | g.23416102C>G | CA389037499 | MHRT,MYH7 | c.4855G>C (p.Glu1619Gln) n.363C>G | |
| 14 | g.23416102C>T | CA015416 | MHRT,MYH7 | c.4855G>A (p.Glu1619Lys) n.363C>T | ClinVar dbSNP |
| 14 | g.23416103C>A | CA389037500 | MHRT,MYH7 | c.4854G>T (p.Met1618Ile) n.364C>A | |
| 14 | g.23416103C>G | CA389037501 | MHRT,MYH7 | c.4854G>C (p.Met1618Ile) n.364C>G | |
| 14 | g.23416103C>T | CA389037502 | MHRT,MYH7 | c.4854G>A (p.Met1618Ile) n.364C>T | |
| 14 | g.23416104A= | CA2123465328 | MHRT,MYH7 | c.4853T= (p.Met1618=) n.365A= | |
| 14 | g.23416104A>C | CA389037503 | MHRT,MYH7 | c.4853T>G (p.Met1618Arg) n.365A>C | |
| 14 | g.23416104A>G | CA389037504 | MHRT,MYH7 | c.4853T>C (p.Met1618Thr) n.365A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416104A>T | CA389037505 | MHRT,MYH7 | c.4853T>A (p.Met1618Lys) n.365A>T | |
| 14 | g.23416104_23416107delinsATCT | CA2123465326 | MHRT,MYH7 | c.4850_4853delinsAGAT (p.Lys1617=) n.365_368delinsATCT | |
| 14 | g.23416105T>A | CA389037506 | MHRT,MYH7 | c.4852A>T (p.Met1618Leu) n.366T>A | |
| 14 | g.23416105T>C | CA389037507 | MHRT,MYH7 | c.4852A>G (p.Met1618Val) n.366T>C | |
| 14 | g.23416105T>G | CA389037508 | MHRT,MYH7 | c.4852A>C (p.Met1618Leu) n.366T>G | |
| 14 | g.23416113_23416115dup | CA2580616566 | MHRT,MYH7 | c.4850_4852dup (p.Lys1617_Met1618insLys) n.374_376dup | ClinVar |
| 14 | g.23416113_23416115del | CA015411 | MHRT,MYH7 | c.4850_4852del (p.Lys1617del) n.374_376del | ClinVar dbSNP |
| 14 | g.23416106C>A | CA389037510 | MHRT,MYH7 | c.4851G>T (p.Lys1617Asn) n.367C>A | |
| 14 | g.23416106C>G | CA389037509 | MHRT,MYH7 | c.4851G>C (p.Lys1617Asn) n.367C>G | |
| 14 | g.23416106C>T | CA485766509 | MHRT,MYH7 | c.4851G>A (p.Lys1617=) n.367C>T | |
| 14 | g.23416107T>A | CA389037511 | MHRT,MYH7 | c.4850A>T (p.Lys1617Met) n.368T>A | |
| 14 | g.23416107T>C | CA389037513 | MHRT,MYH7 | c.4850A>G (p.Lys1617Arg) n.368T>C | |
| 14 | g.23416107T>G | CA389037512 | MHRT,MYH7 | c.4850A>C (p.Lys1617Thr) n.368T>G | |
| 14 | g.23416108T>A | CA389037514 | MHRT,MYH7 | c.4849A>T (p.Lys1617Ter) n.369T>A | |
| 14 | g.23416108T>C | CA389037516 | MHRT,MYH7 | c.4849A>G (p.Lys1617Glu) n.369T>C | |
| 14 | g.23416108T>G | CA389037515 | MHRT,MYH7 | c.4849A>C (p.Lys1617Gln) n.369T>G | |
| 14 | g.23416109C>A | CA389037517 | MHRT,MYH7 | c.4848G>T (p.Lys1616Asn) n.370C>A | |
| 14 | g.23416109C= | CA2123465341 | MHRT,MYH7 | c.4848G= (p.Lys1616=) n.370C= | |
| 14 | g.23416109C>G | CA389037518 | MHRT,MYH7 | c.4848G>C (p.Lys1616Asn) n.370C>G | |
| 14 | g.23416109C>T | CA044065 | MHRT,MYH7 | c.4848G>A (p.Lys1616=) n.370C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416110T>A | CA389037519 | MHRT,MYH7 | c.4847A>T (p.Lys1616Met) n.371T>A | |
| 14 | g.23416110T>C | CA389037521 | MHRT,MYH7 | c.4847A>G (p.Lys1616Arg) n.371T>C | dbSNP |
| 14 | g.23416110T>G | CA389037520 | MHRT,MYH7 | c.4847A>C (p.Lys1616Thr) n.371T>G | |
| 14 | g.23416110T= | CA2123465344 | MHRT,MYH7 | c.4847A= (p.Lys1616=) n.371T= | |
| 14 | g.23416111T>A | CA389037522 | MHRT,MYH7 | c.4846A>T (p.Lys1616Ter) n.372T>A | |
| 14 | g.23416111T>C | CA389037524 | MHRT,MYH7 | c.4846A>G (p.Lys1616Glu) n.372T>C | ClinVar |
| 14 | g.23416111T>G | CA389037523 | MHRT,MYH7 | c.4846A>C (p.Lys1616Gln) n.372T>G | |
| 14 | g.23416112C>A | CA16614393 | MHRT,MYH7 | c.4845G>T (p.Lys1615Asn) n.373C>A | ClinVar dbSNP |
| 14 | g.23416112C= | CA2123465348 | MHRT,MYH7 | c.4845G= (p.Lys1615=) n.373C= | |
| 14 | g.23416112C>G | CA389037525 | MHRT,MYH7 | c.4845G>C (p.Lys1615Asn) n.373C>G | |
| 14 | g.23416112C>T | CA485766510 | MHRT,MYH7 | c.4845G>A (p.Lys1615=) n.373C>T | ClinVar dbSNP |
| 14 | g.23416113T>A | CA389037526 | MHRT,MYH7 | c.4844A>T (p.Lys1615Met) n.374T>A | |
| 14 | g.23416113T>C | CA389037527 | MHRT,MYH7 | c.4844A>G (p.Lys1615Arg) n.374T>C | |
| 14 | g.23416113T>G | CA389037528 | MHRT,MYH7 | c.4844A>C (p.Lys1615Thr) n.374T>G | |
| 14 | g.23416114T>A | CA389037531 | MHRT,MYH7 | c.4843A>T (p.Lys1615Ter) n.375T>A | |
| 14 | g.23416114T>C | CA389037530 | MHRT,MYH7 | c.4843A>G (p.Lys1615Glu) n.375T>C | |
| 14 | g.23416114T>G | CA389037529 | MHRT,MYH7 | c.4843A>C (p.Lys1615Gln) n.375T>G | |
| 14 | g.23416115C>A | CA485766511 | MHRT,MYH7 | c.4842G>T (p.Val1614=) n.376C>A | |
| 14 | g.23416115C>G | CA485766512 | MHRT,MYH7 | c.4842G>C (p.Val1614=) n.376C>G | |
| 14 | g.23416115C>T | CA485766513 | MHRT,MYH7 | c.4842G>A (p.Val1614=) n.376C>T | |
| 14 | g.23416116A= | CA2123465352 | MHRT,MYH7 | c.4841T= (p.Val1614=) n.377A= | |
| 14 | g.23416116A>C | CA389037532 | MHRT,MYH7 | c.4841T>G (p.Val1614Gly) n.377A>C | dbSNP |
| 14 | g.23416116A>G | CA389037533 | MHRT,MYH7 | c.4841T>C (p.Val1614Ala) n.377A>G | |
| 14 | g.23416116A>T | CA389037534 | MHRT,MYH7 | c.4841T>A (p.Val1614Glu) n.377A>T | |
| 14 | g.23416117C>A | CA389037535 | MHRT,MYH7 | c.4840G>T (p.Val1614Leu) n.378C>A | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416117C= | CA2123465356 | MHRT,MYH7 | c.4840G= (p.Val1614=) n.378C= | |
| 14 | g.23416117C>G | CA389037536 | MHRT,MYH7 | c.4840G>C (p.Val1614Leu) n.378C>G | |
| 14 | g.23416117C>T | CA389037537 | MHRT,MYH7 | c.4840G>A (p.Val1614Met) n.378C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416118C>A | CA389037538 | MHRT,MYH7 | c.4839G>T (p.Arg1613Ser) n.379C>A | |
| 14 | g.23416118C= | CA2123465361 | MHRT,MYH7 | c.4839G= (p.Arg1613=) n.379C= | |
| 14 | g.23416118C>G | CA389037539 | MHRT,MYH7 | c.4839G>C (p.Arg1613Ser) n.379C>G | |
| 14 | g.23416118C>T | CA044050 | MHRT,MYH7 | c.4839G>A (p.Arg1613=) n.379C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416119C>A | CA389037540 | MHRT,MYH7 | c.4838G>T (p.Arg1613Met) n.380C>A | |
| 14 | g.23416119C= | CA2123465366 | MHRT,MYH7 | c.4838G= (p.Arg1613=) n.380C= | |
| 14 | g.23416119C>G | CA389037541 | MHRT,MYH7 | c.4838G>C (p.Arg1613Thr) n.380C>G | gnomAD v4 |
| 14 | g.23416119C>T | CA015403 | MHRT,MYH7 | c.4838G>A (p.Arg1613Lys) n.380C>T | ClinVar dbSNP |
| 14 | g.23416120T>A | CA389037542 | MHRT,MYH7 | c.4837A>T (p.Arg1613Trp) n.381T>A | |
| 14 | g.23416120T>C | CA389037543 | MHRT,MYH7 | c.4837A>G (p.Arg1613Gly) n.381T>C | |
| 14 | g.23416120T>G | CA485766514 | MHRT,MYH7 | c.4837A>C (p.Arg1613=) n.381T>G | ClinVar dbSNP |
| 14 | g.23416120T= | CA2123465375 | MHRT,MYH7 | c.4837A= (p.Arg1613=) n.381T= | |
| 14 | g.23416121C>A | CA485766515 | MHRT,MYH7 | c.4836G>T (p.Leu1612=) n.382C>A | |
| 14 | g.23416121C= | CA2123465383 | MHRT,MYH7 | c.4836G= (p.Leu1612=) n.382C= | |
| 14 | g.23416121C>G | CA485766516 | MHRT,MYH7 | c.4836G>C (p.Leu1612=) n.382C>G | gnomAD v4 |
| 14 | g.23416121C>T | CA485766517 | MHRT,MYH7 | c.4836G>A (p.Leu1612=) n.382C>T | dbSNP |
| 14 | g.23416122A= | CA2123465389 | MHRT,MYH7 | c.4835T= (p.Leu1612=) n.383A= | |
| 14 | g.23416122A>C | CA389037544 | MHRT,MYH7 | c.4835T>G (p.Leu1612Arg) n.383A>C | |
| 14 | g.23416122A>G | CA015395 | MHRT,MYH7 | c.4835T>C (p.Leu1612Pro) n.383A>G | ClinVar dbSNP |
| 14 | g.23416122A>T | CA389037545 | MHRT,MYH7 | c.4835T>A (p.Leu1612Gln) n.383A>T | |
| 14 | g.23416123G>A | CA044032 | MHRT,MYH7 | c.4834C>T (p.Leu1612=) n.384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416123G>C | CA015389 | MHRT,MYH7 | c.4834C>G (p.Leu1612Val) n.384G>C | ClinVar dbSNP |
| 14 | g.23416123G= | CA2123465403 | MHRT,MYH7 | c.4834C= (p.Leu1612=) n.384G= | |
| 14 | g.23416123G>T | CA389037546 | MHRT,MYH7 | c.4834C>A (p.Leu1612Met) n.384G>T | |
| 14 | g.23416124G>A | CA485766518 | MHRT,MYH7 | c.4833C>T (p.Ala1611=) n.385G>A | gnomAD v4 |
| 14 | g.23416124G>C | CA485766519 | MHRT,MYH7 | c.4833C>G (p.Ala1611=) n.385G>C | |
| 14 | g.23416124G>T | CA485766520 | MHRT,MYH7 | c.4833C>A (p.Ala1611=) n.385G>T | |
| 14 | g.23416125G>A | CA044022 | MHRT,MYH7 | c.4832C>T (p.Ala1611Val) n.386G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416125G>C | CA389037548 | MHRT,MYH7 | c.4832C>G (p.Ala1611Gly) n.386G>C | |
| 14 | g.23416125G= | CA2123465413 | MHRT,MYH7 | c.4832C= (p.Ala1611=) n.386G= | |
| 14 | g.23416125G>T | CA389037547 | MHRT,MYH7 | c.4832C>A (p.Ala1611Asp) n.386G>T | |
| 14 | g.23416126C>A | CA015382 | MHRT,MYH7 | c.4831G>T (p.Ala1611Ser) n.387C>A | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.23416126C= | CA2123465419 | MHRT,MYH7 | c.4831G= (p.Ala1611=) n.387C= | |
| 14 | g.23416126C>G | CA389037549 | MHRT,MYH7 | c.4831G>C (p.Ala1611Pro) n.387C>G | |
| 14 | g.23416126C>T | CA389037550 | MHRT,MYH7 | c.4831G>A (p.Ala1611Thr) n.387C>T | ClinVar |
| 14 | g.23416127C>A | CA389037551 | MHRT,MYH7 | c.4830G>T (p.Glu1610Asp) n.388C>A | |
| 14 | g.23416127C>G | CA389037552 | MHRT,MYH7 | c.4830G>C (p.Glu1610Asp) n.388C>G | |
| 14 | g.23416127C>T | CA485766521 | MHRT,MYH7 | c.4830G>A (p.Glu1610=) n.388C>T | |
| 14 | g.23416128T>A | CA389037553 | MHRT,MYH7 | c.4829A>T (p.Glu1610Val) n.389T>A | |
| 14 | g.23416128T>C | CA389037554 | MHRT,MYH7 | c.4829A>G (p.Glu1610Gly) n.389T>C | |
| 14 | g.23416128T>G | CA389037555 | MHRT,MYH7 | c.4829A>C (p.Glu1610Ala) n.389T>G | |
| 14 | g.23416128_23416131delinsTCGT | CA2123465429 | MHRT,MYH7 | c.4826_4829delinsACGA (p.Asn1609=) n.389_392delinsTCGT | |
| 14 | g.23416129C>A | CA389037556 | MHRT,MYH7 | c.4828G>T (p.Glu1610Ter) n.390C>A | |
| 14 | g.23416129C= | CA2123465441 | MHRT,MYH7 | c.4828G= (p.Glu1610=) n.390C= | |
| 14 | g.23416129C>G | CA015373 | MHRT,MYH7 | c.4828G>C (p.Glu1610Gln) n.390C>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416129C>T | CA10645050 | MHRT,MYH7 | c.4828G>A (p.Glu1610Lys) n.390C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416129_23416131delinsGGTTGCGGC | CA658658243 | MHRT,MYH7 | c.4826_4828delinsGCCGCAACC (p.Asn1609_Glu1610delinsSerArgAsnGln) n.390_392delinsGGTTGCGGC | ClinVar dbSNP |
| 14 | g.23416130G>A | CA015366 | MHRT,MYH7 | c.4827C>T (p.Asn1609=) n.391G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416130G>C | CA389037558 | MHRT,MYH7 | c.4827C>G (p.Asn1609Lys) n.391G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416130G= | CA2123465452 | MHRT,MYH7 | c.4827C= (p.Asn1609=) n.391G= | |
| 14 | g.23416130G>T | CA389037557 | MHRT,MYH7 | c.4827C>A (p.Asn1609Lys) n.391G>T | gnomAD v4 |
| 14 | g.23416131T>A | CA389037559 | MHRT,MYH7 | c.4826A>T (p.Asn1609Ile) n.392T>A | |
| 14 | g.23416131T>C | CA389037560 | MHRT,MYH7 | c.4826A>G (p.Asn1609Ser) n.392T>C | |
| 14 | g.23416131T>G | CA389037561 | MHRT,MYH7 | c.4826A>C (p.Asn1609Thr) n.392T>G | |
| 14 | g.23416132T>A | CA389037562 | MHRT,MYH7 | c.4825A>T (p.Asn1609Tyr) n.393T>A | |
| 14 | g.23416132T>C | CA389037563 | MHRT,MYH7 | c.4825A>G (p.Asn1609Asp) n.393T>C | |
| 14 | g.23416132T>G | CA389037564 | MHRT,MYH7 | c.4825A>C (p.Asn1609His) n.393T>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416132T= | CA2123465459 | MHRT,MYH7 | c.4825A= (p.Asn1609=) n.393T= | |
| 14 | g.23416133G>A | CA485766522 | MHRT,MYH7 | c.4824C>T (p.Arg1608=) n.394G>A | |
| 14 | g.23416133G>C | CA485766523 | MHRT,MYH7 | c.4824C>G (p.Arg1608=) n.394G>C | |
| 14 | g.23416133G>T | CA485766524 | MHRT,MYH7 | c.4824C>A (p.Arg1608=) n.394G>T | |
| 14 | g.23416134C>A | CA043989 | MHRT,MYH7 | c.4823G>T (p.Arg1608Leu) n.395C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416134C= | CA2123465468 | MHRT,MYH7 | c.4823G= (p.Arg1608=) n.395C= | |
| 14 | g.23416134C>G | CA015359 | MHRT,MYH7 | c.4823G>C (p.Arg1608Pro) n.395C>G | ClinVar dbSNP |
| 14 | g.23416134C>T | CA043977 | MHRT,MYH7 | c.4823G>A (p.Arg1608His) n.395C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |